NIFTY® - Non-Invasive Fetal TrisomY Test

The World’s Leading Non-Invasive Prenatal Test (NIPT)

NIFTY® (Non-Invasive Fetal TrisomY test) is a safe, simple, non-invasive prenatal test (NIPT), which offers screening for certain genetic conditions from as early as week 10 of pregnancy.

Using the latest genetic sequencing technology, NIFTY® has over >99% accuracy for the three most common trisomy conditions present at birth, which are Down Syndrome, Edwards Syndrome and Patau Syndrome.

The Advantages Of The NIFTY® Test

Trusted

Over 9.4 million tests conducted worldwide and validated on a study of over 147,000 pregnancies

Accurate

>99% sensitivity for detection of trisomy conditions such as Down syndrome.

Comprehensive

Screening across all 23 pairs of chromosomes up to 96 genetic conditions

Simple

Test from a small 10 ml maternal blood sample as early as week 10 of pregnancy

Safe

Non-invasive with no risk of miscarriage

Fast

Report delivered within 10 working days

Insured

Offering insurance in cases of false positive or false negative

Workflow

Physician orders test

Blood sample collected

Sample shipped to BGI and analyzed

Results sent to physician

NIFTY test is suitable for

Maternal age 35 years or
older at delivery

Fetal ultrasonographic findings indicating an increased risk of aneuploidy

Require reassurance following previous screening result

Contraindications for invasive prenatal testing, such as placenta prevaria, risk of miscarriage or HBV infection

History of a prior pregnancy with a trisomy

Received IVF Treatment or have previously suffered from habitual abortion

A Comparison of Detection Rates

AVAILABLE FROM WEEK 10 99%
SERUM INTEGRATED SCREENING
AVAILABLE FROM WEEK 15 88%
QUAD SCREENING
AVAILABLE FROM WEEK 15 81%
FIRST TRIMESTER SCREENING
AVAILABLE FROM WEEK 10 80%

Package Test Options

Trisomies
 Trisomy 21 (Down Syndrome)
 Trisomy 18 (Edwards Symdrome)
 Trisomy 13 (Patau Syndrome)
 
Gender Identification
 Male / Female
 
Trisomies
 Trisomy 9
 Trisomy 16
 Trisomy 22
 Other Trisomies
 
Sex Chromosome Aneuploidies
 Monosomy X (Turner syndrome)
 XXY (Klinefelter syndrome)
 XXX (Triple-X)
 XYY (Jacob’s syndrome)
 
Deletion / Duplication
 84 kinds of deletion / duplication
Trisomies
 Trisomy 21 (Down Syndrome)
 Trisomy 18 (Edwards Symdrome)
 Trisomy 13 (Patau Syndrome)
 
Gender Identification
 Male / Female
 
Trisomies
 Trisomy 9
 Trisomy 16
 Trisomy 22
 Other Trisomies
 
Sex Chromosome Aneuploidies
 Monosomy X (Turner syndrome)
 XXY (Klinefelter syndrome)
 XXX (Triple-X)
 XYY (Jacob’s syndrome)
Trisomies
 Trisomy 21 (Down Syndrome)
 Trisomy 18 (Edwards Symdrome)
 Trisomy 13 (Patau Syndrome)
 
Gender Identification
 Male / Female
 
Sex Chromosome Aneuploidies
 Monosomy X (Turner syndrome)
 XXY (Klinefelter syndrome)
 XXX (Triple-X)
 XYY (Jacob’s syndrome)
Trisomies
 Trisomy 21 (Down Syndrome)
 Trisomy 18 (Edwards Symdrome)
 Trisomy 13 (Patau Syndrome)
 
Y Chromosome